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On Commensalism of Candida

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Multi-kingdom gut microbiota analyses define bacterial-fungal interplay and microbial markers of pan-cancer immunotherapy across cohorts

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Bioactive Peptides Against Fungal Biofilms

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Probiotic Yeasts Inhibit Virulence of Non -albicans Candida Species

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Haematopoietic cell transplantation outcomes are linked to intestinal mycobiota dynamics and an expansion of Candida parapsilosis complex species

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Chemical Mediators at the Bacterial-Fungal Interface

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Bacteriocins from lactic acid bacteria and their potential clinical applications

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The interplay between gut bacteria and the yeast Candida albicans

Pérez, J. C. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1979877 · Cited by 74 · see citing works

Heme cross-feeding can augment Staphylococcus aureus and Enterococcus faecalis dual species biofilms

Ch’ng, J.-H., Muthu, M., Chong, K. K. L., Wong, J. J., Tan, C. A. Z., Koh, Z. J. S., López, D., Matysik, A. S., Nair, Z. J., Barkham, T., et al. (2022) · The ISME Journal · doi:10.1038/s41396-022-01248-1 · Cited by 74 · see citing works

Disarming Fungal Pathogens: Bacillus safensis Inhibits Virulence Factor Production and Biofilm Formation by Cryptococcus neoformans and Candida albicans

Mayer, F. L., & Kronstad, J. W. (2017) · mBio · doi:10.1128/mbio.01537-17 · Cited by 76 · see citing works

Candida biofilm production is associated with higher mortality in patients with candidaemia

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Anticandidal Activities by Lactobacillus Species: An Update on Mechanisms of Action

Vázquez-Muñoz, R., & Dongari‐Bagtzoglou, A. I. (2021) · Frontiers in Oral Health · doi:10.3389/froh.2021.689382 · Cited by 71 · see citing works

High-Throughput Screening Identifies Genes Required for Candida albicans Induction of Macrophage Pyroptosis

O’Meara, T. R., Duah, K., Guo, C. X., Maxson, M. E., Gaudet, R. G., Koselny, K., Wellington, M. A., Powers, M. E., MacAlpine, J., O’Meara, M. J., et al. (2018) · mBio · doi:10.1128/mbio.01581-18 · Cited by 67 · see citing works

Application of Probiotic Yeasts on Candida Species Associated Infection

Kunyeit, L., Anu‐Appaiah, K. A., & Rao, R. P. (2020) · Journal of Fungi · doi:10.3390/jof6040189 · Cited by 82 · see citing works

Bacterial‐fungal interactions and their impact on microbial pathogenesis

MacAlpine, J., Robbins, N., & Cowen, L. E. (2022) · Molecular Ecology · doi:10.1111/mec.16411 · Cited by 72 · see citing works

Publisher Correction: The gut–liver axis and the intersection with the microbiome

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Linking Cellular Morphogenesis with Antifungal Treatment and Susceptibility in Candida Pathogens

Sharma, J., Rosiana, S., Razzaq, I., & Shapiro, R. S. (2019) · Journal of Fungi · doi:10.3390/jof5010017 · Cited by 64 · see citing works

Preclinical studies of toxicity and safety of the AS-48 bacteriocin

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The Relationship of Candida albicans with the Oral Bacterial Microbiome in Health and Disease

Bertolini, M., & Dongari‐Bagtzoglou, A. I. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-28524-1_6 · Cited by 61 · see citing works

Mixed biofilms of pathogenic Candida-bacteria: regulation mechanisms and treatment strategies

Khan, F., Bamunuarachchi, N. I., Pham, D. T. N., Tabassum, N., Khan, M. S., & Kim, Y. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1921696 · Cited by 61 · see citing works

Pathogenetic Impact of Bacterial–Fungal Interactions

Nogueira, F., Sharghi, S., Kuchler, K., & Lion, T. (2019) · Microorganisms · doi:10.3390/microorganisms7100459 · Cited by 57 · see citing works

Interactions between Candida albicans and the resident microbiota

Li, H., Miao, M., Jia, C., Cao, Y.-B., Yan, T., Jiang, Y., & Yang, F. J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.930495 · Cited by 58 · see citing works

Caenorhabditis elegans in high-throughput screens for anti-infective compounds

Peterson, N., & Pukkila-Worley, R. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.06.003 · Cited by 53 · see citing works

The gut commensal bacterium Enterococcus faecalis LX10 contributes to defending against Nosema bombycis infection in Bombyx mori

Zhang, X., Feng, H., He, J., Liang, X., Zhang, N., Shao, Y., Zhang, F., & Lu, X. (2022) · Pest Management Science · doi:10.1002/ps.6846 · Cited by 54 · see citing works

Antifungal therapy of Candida biofilms: Past, present and future

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Candida–bacterial cross-kingdom interactions

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Lactobacillus paracasei 28.4 reduces in vitro hyphae formation of Candida albicans and prevents the filamentation in an experimental model of Caenorhabditis elegans

de Barros, P. P., Scorzoni, L., Ribeiro, F. D. C., Fugisaki, L. R. D. O., Fuchs, B. B., Mylonakis, E. E., Jorge, A. O. C., Junqueira, J. C., & Rossoni, R. D. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.02.019 · Cited by 53 · see citing works

Bacterial Vaginosis and Vulvovaginal Candidiasis Pathophysiologic Interrelationship

Sobel, J. D., & Vempati, Y. S. (2024) · Microorganisms · doi:10.3390/microorganisms12010108 · Cited by 56 · see citing works

Klebsiella pneumoniae prevents spore germination and hyphal development of Aspergillus species

Nogueira, F., Pereira, L., Jenull, S., Kuchler, K., & Lion, T. (2019) · Scientific Reports · doi:10.1038/s41598-018-36524-8 · Cited by 50 · see citing works

Antibiofilm Efficacy of Luteolin Against Single and Dual Species of Candida albicans and Enterococcus faecalis

Fu, Y., Wang, W., Zeng, Q., Wang, T., & Qian, W. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.715156 · Cited by 49 · see citing works

Antifungal activity of the Enterococcus faecalis peptide EntV requires protease cleavage and disulfide bond formation

Brown, A. O., Graham, C. E., Cruz, M. R., Singh, K. V., Murray, B. E., Lorenz, M. C., & Garsin, D. A. (2019) · mBio · doi:10.1128/mbio.01334-19 · Cited by 46 · see citing works

Yeast and Filaments Have Specialized, Independent Activities in a Zebrafish Model of Candida albicans Infection

Seman, B. G., Moore, J. L., Scherer, A. K., Blair, B. A., Manandhar, S., Jones, J. M., & Wheeler, R. T. (2018) · Infection and Immunity · doi:10.1128/iai.00415-18 · Cited by 44 · see citing works

The Increasing Issue of Vancomycin-Resistant Enterococci and the Bacteriocin Solution

Reinseth, I. S., Ovchinnikov, K. V., Tønnesen, H. H., Carlsen, H., & Diep, D. B. (2019) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-019-09618-6 · Cited by 48 · see citing works

Candida albicans can foster gut dysbiosis and systemic inflammation during HIV infection

Zaongo, S. D., Ouyang, J., Isnard, S., Zhou, X., Harypursat, V., Cui, H., Routy, J., & Chen, Y. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2167171 · Cited by 47 · see citing works

Candida–Bacterial Biofilms and Host–Microbe Interactions in Oral Diseases

Negrini, T. D. C., Koo, H., & Arthur, R. A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-28524-1_10 · Cited by 44 · see citing works

Skin-associated lactic acid bacteria from North American bullfrogs as potential control agents of Batrachochytrium dendrobatidis

Niederle, M. V., Bosch, J., Ale, C. E., Nader-Macı́as, M. E., Ficoseco, C. A., Toledo, L. F., Valenzuela‐Sánchez, A., Azat, C., & Pasteris, S. E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223020 · Cited by 42 · see citing works

Opportunistic yeast pathogen Candida spp.: Secreted and membrane-bound virulence factors

Lim, S. J., Ali, M. S. M., Sabri, S., Noor, N. D. M., Salleh, A. B., & Oslan, S. N. (2021) · Medical Mycology · doi:10.1093/mmy/myab053 · Cited by 41 · see citing works

ADH1 promotes Candida albicans pathogenicity by stimulating oxidative phosphorylation

Song, Y., Li, S., Zhao, Y., Zhang, Y., Lv, Y., Jiang, Y., Wang, Y., Li, D., & Zhang, H. (2019) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2019.151330 · Cited by 41 · see citing works

Caenorhabditis elegans as a model animal for investigating fungal pathogenesis

Madende, M., Albertyn, J., Sebolai, O. M., & Pohl, C. H. (2019) · Medical Microbiology and Immunology · doi:10.1007/s00430-019-00635-4 · Cited by 41 · see citing works

Binary interactions between the yeast Candida albicans and two gut-associated Bacteroides species

Valentine, M., Benadé, E., Mouton, M., Khan, W., & Botha, A. (2019) · Microbial Pathogenesis · doi:10.1016/j.micpath.2019.103619 · Cited by 40 · see citing works

Bioactive triterpenoids from Solanum torvum fruits with antifungal, resistance modulatory and anti-biofilm formation activities against fluconazole-resistant candida albicans strains

Harley, B. K., Neglo, D., Tawiah, P. A., Pipim, M. A., Mireku-Gyimah, N. A., Tettey, C. O., Amengor, C. D. K., Fleischer, T. C., & Waikhom, S. D. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260956 · Cited by 40 · see citing works

Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model

Krishnamoorthy, A. L., Lemus, A. A., Solomon, A. P., Valm, A. M., & Neelakantan, P. (2020) · Microorganisms · doi:10.3390/microorganisms8111771 · Cited by 37 · see citing works

Bacteriocin—a potential antimicrobial peptide towards disrupting and preventing biofilm formation in the clinical and environmental locales

Duraisamy, S., Balakrishnan, S., Ranjith, S., Husain, F., Sathyan, A., Peter, A. S., Prahalathan, C., & Kumarasamy, A. (2020) · Environmental Science and Pollution Research · doi:10.1007/s11356-020-10989-5 · Cited by 37 · see citing works

The interactions of Candida albicans with gut bacteria: a new strategy to prevent and treat invasive intestinal candidiasis

Fei, W., Wang, Z., & Tang, J. (2023) · Gut Pathogens · doi:10.1186/s13099-023-00559-8 · Cited by 34 · see citing works

Coexistence of Candida albicans and Enterococcus faecalis increases biofilm virulence and periapical lesions in rats

Du, Q., Yuan, S., Zhao, S., Fu, D., Chen, Y., Zhou, Y., Cao, Y., Gao, Y., Xu, X., Zhou, X., et al. (2021) · Biofouling · doi:10.1080/08927014.2021.1993836 · Cited by 35 · see citing works

Candida albicans dwelling in the mammalian gut

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Dispersal and inhibition of biofilms associated with infections

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Fungi at the Scene of the Crime: Innocent Bystanders or Accomplices in Oral Infections?

Delaney, C., Kean, R., Short, B., Tumelty, M., McLean, W., Nile, C. J., & Ramage, G. (2018) · Current Clinical Microbiology Reports · doi:10.1007/s40588-018-0100-3 · Cited by 33 · see citing works

Co‐ and polymicrobial infections in the gut mucosa: The host–microbiota–pathogen perspective

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Orodispersible Film Loaded with Enterococcus faecium CRL183 Presents Anti-Candida albicans Biofilm Activity In Vitro

Lordello, V. B., Meneguin, A. B., de Annunzio, S. R., Taranto, M. P., Chorilli, M., Fontana, C. R., & Cavallini, D. C. U. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13070998 · Cited by 32 · see citing works

Symbiosis and Dysbiosis of the Human Mycobiome

Mishra, K., Bukavina, L., & Ghannoum, M. A. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.636131 · Cited by 32 · see citing works

Structural and functional analysis of EntV reveals a 12 amino acid fragment protective against fungal infections

Cruz, M. R., Cristy, S., Guha, S., De Cesare, G. B., Evdokimova, E., Sanchez, H., Borek, D., Miramón, P., Yano, J., Fidel, P. L., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33613-1 · Cited by 30 · see citing works

Exploring the frontiers of therapeutic breadth of antifungal peptides: A new avenue in antifungal drugs

Haq, I. U., Maryam, S., Shyntum, D. Y., Khan, T. A., & Li, F. (2024) · Journal of Industrial Microbiology & Biotechnology · doi:10.1093/jimb/kuae018 · Cited by 30 · see citing works

The Skin Commensal Yeast Malassezia globosa Thwarts Bacterial Biofilms to Benefit the Host

Ianiri, G., Heitman, J., & Scheynius, A. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.01.008 · Cited by 30 · see citing works

Promising Anti-Biofilm Agents and Phagocytes Enhancers for the Treatment of Candida albicans Biofilm–Associated Infections

Tartor, Y. H., Elmowalid, G. A., Hassan, M. N., Shaker, A., Ashour, D. F., & Saber, T. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.807218 · Cited by 30 · see citing works

Doderlin: isolation and characterization of a broad-spectrum antimicrobial peptide from Lactobacillus acidophilus

da Silva, B. S., Díaz-Roa, A., Yamane, E. S., Hayashi, M. A. F., & da Silva, P. I. (2022) · Research in Microbiology · doi:10.1016/j.resmic.2022.103995 · Cited by 29 · see citing works

A Toll pathway effector protects Drosophila specifically from distinct toxins secreted by a fungus or a bacterium

Huang, J., Lou, Y., Liu, J., Bulet, P., Cai, C., Ma, K., Jiao, R., Hoffmann, J. A., Liégeois, S., Li, Z., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2205140120 · Cited by 30 · see citing works

Candida albicans and Enterococcus faecalis biofilm frenemies: When the relationship sours

Alshanta, O. A., Albashaireh, K. Z., McKloud, E., Delaney, C., Kean, R., McLean, W., & Ramage, G. (2022) · Biofilm · doi:10.1016/j.bioflm.2022.100072 · Cited by 29 · see citing works

Membrane Permeabilization and Antimicrobial Activity of Recombinant Defensin-d2 and Actifensin against Multidrug-Resistant Pseudomonas aeruginosa and Candida albicans

Gbala, I., Macharia, R. W., Bargul, J. L., & Magoma, G. N. (2022) · Molecules · doi:10.3390/molecules27144325 · Cited by 28 · see citing works

Commensal yeast promotes Salmonella Typhimurium virulence

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Intestinal bacteria—a powerful weapon for fungal infections treatment

Cong, L., Chen, C., Mao, S., Han, Z., Zhu, Z., & Li, Y. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1187831 · Cited by 29 · see citing works

In Vitro Antibiofilm and Anti-Inflammatory Properties of Bacteriocins Produced by Pediococcus acidilactici Against Enterococcus faecalis

Yoon, J.-W., & Kang, S. (2020) · Foodborne Pathogens and Disease · doi:10.1089/fpd.2020.2804 · Cited by 27 · see citing works

Parental Care Alters the Egg Microbiome of Maritime Earwigs

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Analyzing the human gut mycobiome – A short guide for beginners

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Pseudogymnoascus destructans growth in wood, soil and guano substrates

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Nisin Production by Enterococcus hirae DF105Mi Isolated from Brazilian Goat Milk

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Cardiac Microlesions Form During Severe Bacteremic Enterococcus faecalis Infection

Brown, A. O., Singh, K. V., Cruz, M. R., Kaval, K. G., Francisco, L. E., Murray, B. E., & Garsin, D. A. (2020) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaa371 · Cited by 24 · see citing works

Characterization of an allosteric inhibitor of fungal-specific C-24 sterol methyltransferase to treat Candida albicans infections

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Interactions between invasive fungi and symbiotic bacteria

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Understanding Human Microbiota Offers Novel and Promising Therapeutic Options against Candida Infections

Hameed, S., Hans, S., Monasky, R. C., Thangamani, S., & Fatima, Z. (2021) · Pathogens · doi:10.3390/pathogens10020183 · Cited by 23 · see citing works

Novel Chronic Wound Healing by Anti-biofilm Peptides and Protease

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Effects of arsenic on the biofilm formations of arsenite-oxidizing bacteria

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Swapping the roles of bacteriocins and bacteriophages in food biotechnology

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Mechanisms of Candida Resistance to Antimycotics and Promising Ways to Overcome It: The Role of Probiotics

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MECHANISM OF CANDIDA ALBICANS BIOFILM AND VIRULENCE INHIBITION BY A BACTERIAL SECRETED FACTOR

Graham, C. E. (2017) · Digital Commons-TMC (Texas Medical Center)

Culture Supernatant of Enterococcus faecalis Promotes the Hyphal Morphogenesis and Biofilm Formation of Candida albicans

Jiang, Q., Jing, Q., Ren, B., Cheng, L., Zhou, X., Lai, W., He, J., & Li, M. (2022) · Pathogens · doi:10.3390/pathogens11101177 · Cited by 15 · see citing works

Enterococcus faecalis Cell-Free Supernatant Inhibits Hyphal Morphogenesis and Biofilm Formation in Candida albicans

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Enterococcus faecalis inhibits hyphal morphogenesis and virulence of Candida albicans

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Virulence And Biofilm Formation In Candida Albicans Are Inhibited By Short Peptide Subunits Of Entv

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